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The connexin 30 A88V mutant reduces cochlear gap junction expression and confers long-term protection against hearing loss.

Kelly JJ, Abitbol JM, Hulme S, Press ER, Laird DW, Allman BL. Kelly JJ, et al. Among authors: press er. J Cell Sci. 2019 Jan 16;132(2):jcs224097. doi: 10.1242/jcs.224097. J Cell Sci. 2019. PMID: 30559251

Induction of cell death and gain-of-function properties of connexin26 mutants predict severity of skin disorders and hearing loss.

Press ER, Shao Q, Kelly JJ, Chin K, Alaga A, Laird DW. Press ER, et al. J Biol Chem. 2017 Jun 9;292(23):9721-9732. doi: 10.1074/jbc.M116.770917. Epub 2017 Apr 20. J Biol Chem. 2017. PMID: 28428247 Free PMC article.

Mutant Cx30-A88V mice exhibit hydrocephaly and sex-dependent behavioral abnormalities, implicating a functional role for Cx30 in the brain.

Novielli-Kuntz NM, Press ER, Barr K, Prado MAM, Laird DW. Novielli-Kuntz NM, et al. Among authors: press er. Dis Model Mech. 2021 Jan 26;14(1):dmm046235. doi: 10.1242/dmm.046235. Dis Model Mech. 2021. PMID: 33735099 Free PMC article.

Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.

Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW. Press E, et al. Cell Death Dis. 2017 Jun 1;8(6):e2845. doi: 10.1038/cddis.2017.234. Cell Death Dis. 2017. PMID: 28569788 Free PMC article.

Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.

Press E, Alaga KC, Barr K, Shao Q, Bosen F, Willecke K, Laird DW. Press E, et al. Cell Death Dis. 2018 May 24;9(6):630. doi: 10.1038/s41419-018-0639-1. Cell Death Dis. 2018. PMID: 29795380 Free PMC article.

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